Variant report

Variant rs10767705
Chromosome Location chr11:28264341-28264342
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:28232200-28268600 Weak transcription Duodenum Mucosa Duodenum
2 chr11:28234400-28266600 Weak transcription Primary B cells from cord blood blood
3 chr11:28251400-28278600 Weak transcription Primary hematopoietic stem cells blood
4 chr11:28251400-28279600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr11:28251400-28297600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr11:28260600-28269600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr11:28263400-28266400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr11:28263400-28269800 Weak transcription Psoas Muscle Psoas
9 chr11:28263400-28279800 Weak transcription Ovary ovary
10 chr11:28264000-28267000 Enhancers NHDF-Ad bronchial
11 chr11:28264200-28264400 Enhancers Aorta Aorta
12 chr11:28264200-28264800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr11:28264200-28265400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr11:28264200-28265600 Enhancers HSMM muscle
15 chr11:28264200-28266000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr11:28264200-28266600 Enhancers Osteobl bone
17 chr11:28264200-28267400 Enhancers Muscle Satellite Cultured Cells --
18 chr11:28264200-28282800 Weak transcription Pancreas Pancrea

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